Primary Device ID | G589EZ2K2 |
NIH Device Record Key | 540db021-0425-438e-a013-67d8966931ae |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | EZPRF |
Version Model Number | EZ2K |
Catalog Number | EZ2K |
Company DUNS | 015144539 |
Company Name | CosmoFrance |
Device Count | 2 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | true |
Device Combination Product | false |
Single Use | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | true |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | true |
RX Perscription | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
HIBCC | D20230209 [Unit of Use] |
HIBCC | G589EZ2K2 [Primary] |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-03-04 |
Device Publish Date | 2024-02-23 |
D20230209 | EZ4K |
G589EZ2K2 | EZ2K |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
EZPRF 87379013 5638636 Live/Registered |
ECTODERMA INC 2017-03-21 |